Evidence map›Paper›PMID 41639876›Full record

ArticleJournal of pharmaceutical health care and sciences2026

Day 8 monocyte and lymphocyte counts as a novel and early predictor for discontinuation in gynecologic cancer patients receiving paclitaxel and carboplatin therapy: a retrospective observational study.

Hiroaki Watanabe, Keita Hirai, Hirofumi Komachiya, Takafumi Naito

Abstract read
In one paragraph

Article in Journal of pharmaceutical health care and sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hiroaki WatanabeDepartment of Pharmacy, Shinshu University Hospital, 3-1-1 Asahi, Matsumoto, Nagano, 390-8621, Japan. hwatanabe@p.kanazawa-u.ac.jp.
Keita HiraiDepartment of Pharmacy, Shinshu University Hospital, 3-1-1 Asahi, Matsumoto, Nagano, 390-8621, Japan. hiraik@shinshu-u.ac.jp.
Hirofumi KomachiyaDepartment of Pharmacy, Showa Inan General Hospital, Akaho 3230, Komagane, Nagano, 399-4117, Japan.
Takafumi NaitoDepartment of Pharmacy, Shinshu University Hospital, 3-1-1 Asahi, Matsumoto, Nagano, 390-8621, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMaintaining optimal treatment intensity is essential for therapeutic efficacy in gynecological malignancies undergoing paclitaxel plus carboplatin (TC) chemotherapy; however, myelosuppression frequently results in treatment delay or interruption, which can compromise long-term outcomes. While previous research has predominantly focused on pre-treatment laboratory values and late-onset adverse events, there is a crucial gap in identifying early, actionable biomarkers. This study sought to evaluate the utility of post-treatment values measured at an early time point (Day 8) to facilitate timely and proactive supportive interventions.

methodsThis retrospective analysis included 242 patients who underwent TC chemotherapy. Patients who discontinued therapy for reasons other than myelosuppression (e.g., allergic reactions or patient choice) were excluded from the final analyses. The primary outcome was treatment interruption (delay or cessation) due to persistence of myelosuppression during the first cycle. Predictive modeling assessed baseline, day 8, and combined hematological factors (including neutrophil, monocyte, and lymphocyte counts, and their derived ratios). Predictive performance was evaluated using multivariate logistic regression and receiver operating characteristic (ROC) curve analyses.

resultsThe model incorporating both pre- and post-treatment laboratory values demonstrated superior predictive performance, evidenced by a significantly higher area under the ROC curve than the model utilizing only pre-treatment factors (0.82 vs. 0.73, P = 0.011). Decision tree analysis identified critical cutoff points for post-treatment laboratory values: monocyte counts below 51/µL and lymphocyte counts below 994/µL on day 8 after chemotherapy. Additionally, a pre-treatment neutrophil count of 2,795/µL was identified as a significant risk factor.

conclusionsEarly post-treatment hematological indices, particularly the day 8 monocyte and lymphocyte counts, were identified as more robust predictors of chemotherapy interruption due to myelosuppression, in addition to pre-treatment indices. These findings suggest that routine monitoring and proactive supportive interventions guided by these specific early post-treatment markers should be implemented in clinical pharmacy practice to enhance treatment continuity and optimize patient outcomes.

Indexed as

CarboplatinGynecological cancerMyelosuppressionPaclitaxelRisk factor

Identifiers

PMID41639876
PMCPMC12964638

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.